Skip to main content
. 2020 Mar 18;2020(3):CD013559. doi: 10.1002/14651858.CD013559

ChiCTR1800019782.

Trial name or title The effect of Intense pulsed light on moderate meibomian gland dysfunction
Methods Study design: randomised controlled trial
Study grouping: parallel group
Exclusions after randomisation? Not applicable
Percentage of participant follow‐up: not applicable
Study duration (of intervention): not reported
Was a sample size calculation reported: no
Participants Baseline characteristics
IPL + MGX group
  • Number of participants (number of eyes): 30 (not reported)

  • Sex: not reported

  • Age: not reported


MGX (standard therapy) group
  • Number of participants (number of eyes): 30

  • Sex: not reported

  • Age: not reported


Overall
  • Number of participants (number of eyes): 60 (not reported)

  • Sex: not reported

  • Age: not reported


Inclusion criteria: aged ≥ 18 years; SPEED score ≥ 6 points; eyelid margin obtuse or hypertrophy or new blood vessels; meibomian gland orifices obstruction, uplift or lipid suppository form; meibum quality score of a single eyelid 5–10 points; Schimer test > 5 mm
Exclusion criteria: eye infection, surgery or trauma in past 6 months; eyelid closure insufficiency, entropion or ectropion, etc.; Fitzpatrick skin category 5–6; treatment before 4 weeks with a tan or tanning, tender skin treatment or have been too sensitive or allergic symptoms; pretreatment area is skin cancer or pigmentary lesions; in past month have dry eye physical therapy or point with anti‐inflammatory drugs; systemic immune‐related diseases, such as Sjogren's syndrome, Stevens‐Johnson syndrome, rheumatism, etc.; nerve lesions, such as trigeminal nerve tumours, surgery or trauma, virus damage, etc.; people with metabolic diseases such as diabetes mellitus, hypothyroidism and thyroid hyperfunction, etc.
Significant pretreatment baseline differences? Not applicable
Severity of dry eye: not reported
Interventions IPL + MGX
  • Description: 520 nm IPL + MGX

  • Duration: not reported

  • Co‐interventions: not reported


Standard therapy only
  • Description: MGX

  • Duration: not reported

  • Co‐interventions: not reported

Outcomes Primary outcomes:
  • SPEED score

  • blepharoplasty score

  • location of Marx line

  • inflammatory factors expression in ocular surface

Starting date Recruiting status: recruiting (as of 18 September 2019)
Contact information Study leader: Zeng Qingyan
Hankou Aier Eye Hospital, 328 Machang Road, Jianghan District, Wuhan, Hubei, China
Email: zengqingyan1972@163.com
Telephone: +86 13971009610
Notes None